Canonical Allele Identifier: CA2245716626
Gene: ACADVL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7225096G= , CM000679.2:g.7225096G= GRCh38
NC_000017.10:g.7128415G= , CM000679.1:g.7128415G= GRCh37
NC_000017.9:g.7069139G= NCBI36
NG_007975.1:g.10263G=
NG_033038.1:g.14449C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356839.10:c.1967G= MANE Select ENSP00000349297.5:p.Ter656=
ENST00000322910.9:c.*1922G= ENSP00000325395.5:n.*1922G=
ENST00000350303.9:c.1901G= ENSP00000344152.5:p.Ter634=
ENST00000356839.9:c.1967G= ENSP00000349297.5:p.Ter656=
ENST00000542255.6:c.846G=
ENST00000543245.6:c.2036G= ENSP00000438689.2:p.Ter679=
ENST00000578033.1:n.392G=
ENST00000578319.5:n.548G=
ENST00000578711.1:n.1592G=
ENST00000578809.5:n.539G=
ENST00000579425.5:n.1083G=
ENST00000583848.5:c.333G= ENSP00000466487.1:n.333G=
ENST00000583850.5:n.738G=
ENST00000583858.5:c.898G=
NM_000018.3:c.1967G= NP_000009.1:p.Ter656=
NM_001033859.2:c.1901G= NP_001029031.1:p.Ter634=
NM_001270447.1:c.2036G= NP_001257376.1:p.Ter679=
NM_001270448.1:c.1739G= NP_001257377.1:p.Ter580=
XM_006721516.2:c.1988G= XP_006721579.2:p.Ter663=
XM_011523829.1:c.1886G= XP_011522131.1:p.Ter629=
XM_011523830.1:c.1865G= XP_011522132.1:p.Ter622=
XR_934021.1:n.2070G=
XR_934022.1:n.1976G=
XR_934023.1:n.1997G=
XM_006721516.3:c.1988G= XP_006721579.2:p.Ter663=
XM_011523829.2:c.1886G= XP_011522131.1:p.Ter629=
XM_011523830.2:c.1865G= XP_011522132.1:p.Ter622=
XM_024450741.1:c.1955G= XP_024306509.1:p.Ter652=
XR_934021.2:n.2022G=
XR_934022.2:n.1928G=
XR_934023.2:n.1949G=
NM_000018.4:c.1967G= MANE Select NP_000009.1:p.Ter656=
NM_001033859.3:c.1901G= NP_001029031.1:p.Ter634=
NM_001270447.2:c.2036G= NP_001257376.1:p.Ter679=
NM_001270448.2:c.1739G= NP_001257377.1:p.Ter580=